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By Hong Yong Sohn

On the occasion of this symposium in my name, I reflect upon the contributions of my academic mentors and early associates who helped shape my professional career. I was fortunate to have these people around me during my graduate work and at the start of my professional career. In forming my view of the technical field and career, they represented academia, research institutions, industry, and different parts of the world.

Jan 1, 2006

By Hong Yong Sohn

On the occasion of this symposium in my name, I reflect upon the contributions of my academic mentors and early associates who helped shape my professional career. I was fortunate to have these people around me during my graduate work and at the start of my professional career. In forming my view of the technical field and career, they represented academia, research institutions, industry, and different parts of the world.

Jan 1, 2006

By Alexandr I. Volkhin

It is practically useful to separate copper from nickel at the fire refining stage of blister copper by transferring nickel in electrochemical inert silicides which are being concentrated further into the tank-house slimes. The treatment of copper melt by silicon-containing reagents is resulted in lowering the interfacial tension of the melt, its deoxidizing, selective siliconizing of in-melt nickel and forming a by-product with fluxing properties. Si-containing reagents have positive influence on results of fire and electrolytic refining, and further pulverizing of copper in plant conditions.

Jan 1, 2006

By M. L. Free

Electrowinning is directly impacted by many parameters that include electrolyte composition, voltage, current density, contact resistance, temperature, electrode spacing, and fluid flow as well as many other interrelated factors. The effects of these parameters are primarily related to thermodynamics, mass transport, and electrochemical kinetics. In this study thermodynamic, mass transport, and electrochemical kinetic equations are simultaneously solved to determine the effects of such parameters on electrowinning current efficiency, power consumption, electrodeposit morphology, and electrodeposit distribution. Modeling predictions will be compared with experimental results.

Jan 1, 2006

By Chen Ya

Layered LiMn0.5Ni0.3Co0.2O2 was prepared from Mn(NO3)2, Ni(NO3)2, Co(NO3)2 and LiOH by co-precipitation and solid state reaction. XRD, C-V and galvanostatic charge-discharge methods were used to examine the structural and electrochemical characteristics. The LiMn0.5Ni0.3Co0.2O2 delivered a high discharge capacity of 167 mAh/g between 2.5 and 4.3 V with excellent cycling stability.

Jan 1, 2006

By Iain B. Mackenzie

In 1997, a thin layer of Microtherm Microporous Insulation was used to replace fireclay brick behind the magnesia/chrome working lining in #5 refining furnace at BHP?s San Manuel AZ smelter. A 23°C reduction in shell temperature was obtained, together with a large increase in the working capacity of the vessel. There was no sign of metal penetration as a result of the increased insulation. Following these highly favorable results, BHP have introduced this product into all of their refining furnaces.

Jan 1, 1999

By Beatriz Ramírez

Xanthates are anionic collectors normally used in flotation devices to modify the hydrophobic surface of sulphide minerals. Xanthates are heteropolar compounds and in aqueous media they dissociate into ionic xanthate and alkali-metal ions; nevertheless their behaviour is not well understood yet. This work characterises the six reactions describing the decomposition of the ionic xanthate in aqueous media by analysing the set of spectra from a UV- Spectrophotometer. Results show the effect of pH on the stability of certain compounds which can be useful to explain the relationships among xanthates and the hidrophobicity of some surfaces (or ions dissolved).

Jan 1, 2006

By Steven Wright

The extent and the rate of reduction of slags produced from the smelting of recycled lead batteries were investigated under laboratory conditions using graphite as reductant. Simultaneous reduction of PbO, Fe2O3, Sb2O3 and As2O3 occurred at temperatures of 1180 and 1200°C, with Sb and As reporting to the metal phase while the PbO content of the slag was above 2 wt%. Fuming of As from the metal occurred at lower concentrations of lead in the slag. Discard slags with low levels of As, Pb and Sb were produced. Arsenic levels were reduced to less than accurately measurable by ICP analysis, and Sb levels in the final slags were in the range of 0.1 to 0.2 wt%. The kinetic data obtained were analysed and compared with other measurements on lead oxide containing slags. The results showing a dependence of the reduction rate on the oxidation state and the basicity are consistent with other studies on well characterised industrial and. synthetic lead slags. These results indicate that when carbonaceous reductants are used, the rate of interfacial reactions play an important role in enabling the production of environmentally acceptable discard slags.

Jan 1, 1994

By E. Salinas-Rodriguez, J. Hernández-Ávila, E. O. Ávila-Dávila, A. Romero-Serrano, M. Perez-Labra, G. Juárez-López

"Single phase rubidium jarosite was synthesized by precipitation from aqueous solution. X-ray diffraction and SEM-EDS analyses showed that the synthetic rubidium jarosite formed in subspherical particles with an average particle size of about 35 µm. The chemical analysis showed an approximate composition of Rbo9432Fe3(SO4)2 1245(OH)6. The decomposition behaviour of the jarosite in terms of solution pH was thermodynamically modeled using FACTSage by constructing the potential-pH diagram at 298.15 K. The E-pH diagram showed that the decomposition of jarosite leads to goethite (FeOOH) together with Rb+ and SO42- ions. The experimental decomposition of the Rb-jarosite was carried out in alkaline solutions with five different Ca(OH)2 concentrations. The decomposition process showed an ""induction period"" followed y a progressive conversion period where the Rb+ and SO42- ions formed in the aqueous solution. In contrast, calcium was incorporated in the solid residue and iron was transformed into amorphous ferrihydrite. The kinetic analysis showed that this process can be represented by the unreacted-core chemically controlled model. The reaction order with respect to Ca(OH)2 is 0.4342 and the calculated activation energy is 98.70 kJ mol-1. IntroductionJarosite type compounds are hydrous sulfate minerals containing alkalis and ferric ions, MFe3(SO4)2(OH)6, where M can be H3O+· Na+, K+, Rb+, Ag+, NH4 +, Tl+, ½ Pb2+ or ½ Hg2+. Jarosite-type compounds were formed by the natural ""in situ"" oxidation of pyritic ores leading to the replacement of the original iron sulfides and iron oxides (Dutrizac and Kaiman) [1]. The great interest in jarosites is due to its ability to eliminate or diminish the iron concentration of the acid leach solutions produced in the hydrometallurgical zinc process, with relatively low losses of divalent metals such as Zn2+, Cd2+, Cu2+ or Co . However, the losses of the metal values demand a careful study of the conditions under which the jarosite compounds are formed together with their chemical properties."

Jan 1, 2012

By Akram Alfantzai, Farzad Mohammadi, Maysam Mohammadi

"Degradation of lead anodes has always been a major concern among the electrowinning industries. In this study, the effect of agitation of the zinc electrowinning solution on the integrity of lead anodes was investigated. Galvanostatic experiments were performed at 37±0.5°C using 0,600 and l000rpm magnetic stirring rates for 24 hours. The Pb02 layer formed on the anode surface was reduced to PbS04 (discharged). The discharge information was used to calculate the amount of Pb02 present on the surface. Weight loss measurements along with the discharge calculations revealed that the degradation rate of the lead anode increased as the solution was stirred more vigorously. Furthermore, the amount of remaining Pb02 on the surfaces was decreased as a function of solution velocity. Therefore, it may be concluded that, degradation rate oflead anodes is controlled by detachment of the corrosion products from the surface rather than by electrochemical reactions. IntroductionElectrowinning is one of the extraction stages of zinc, in which pure zinc is deposited from acidic solution after froth flotation, roasting and leaching processes. The anode electrode materials play important roles in the electrowinning process. Their electrocatalytical capacities determine the oxygen evolution overpotential, and consequently the cell potential and energy efficiency of the zinc electrodeposition [l]. Purity of the zinc deposited on the cathode is affected by the solubility and corrosion resistance of the anode materials. Using insoluble materials as anode in the electrowinning leads to the higher purity of the deposited metal on the cathode[2]. Lead (Pb) and its alloys have been used as the anode in the zinc electrowinning because of its special properties such as relatively low cost, low melting point, insolubility in solutions containing sulphuric acid and high conductivity in both states of metallic and oxidized [3, 4]. In zinc electrowinnig, zinc reduction occurs on the cathode (reaction 1) and the oxygen evolution reaction (OER) (reaction 2) is the main anodic reaction [5, 6]."

Jan 1, 2013

By Heinz Boeni, Daniel Ott, Uca Silva

"Latin America is facing a rapid increase in internet use. Penetration with electronic equipment is in some countries approaching the level of industrialized countries. There is an evident need to resolve the management of “end-of-life” computers and other electronic equipment. Several studies in Latin America assessed the increasing e-waste quantities and confirmed the importance of a sustainable e-waste management. This paper gives an overview on the status on e-waste management in Latin America, explains the challenges for establishing an e-waste management system in a developing country setting and highlights the social and economic potential and the possibilities of a regional approach.IntroductionGlobal ICT-Trade and generation of e-waste from ICTThe global production of electronic devices and particularly of Information and Communication Technologies (ICT) faces the biggest industrial expansion of the history: OECD figures show that global trade of ICT technologies has reached 7.7% of the gross world product by 2004, the major proportion accruing from China [1]. In 2006 an estimated 230 million computers and 1 billion cell phones have been sold worldwide which corresponds to a volume of 5’848’000 t [2]. As a consequence, Waste from Electrical and Electronic Equipment (WEEE), or e-waste, is by far the fastest growing waste component. It reaches more than 5% referred to Municipal Solid Waste and e-waste generation in developing countries according to UNEP is expected to triple by 2010 [2].According to the OECD e-waste is “any appliance using an electric power supply that has reached its end-of-life” [3]. The European WEEE directive [4] distinguishes 10 categories of ewaste: Big household appliances, Small Household Appliances, IT and Telecommunications Equipment, Consumer Equipment, Lighting Equipment, Electrical and Electronic Tools, Toys, Leisure and Sports Equipment, Medical devices, Monitoring and Control Instruments, and Automatic dispensers. In this paper e-waste and WEEE are used as synonyms. Focus will be laid on e-waste from IT equipment (IT-waste), corresponding to category 3 of the European WEEEDirective."

Jan 1, 2008

By Shuo Wang, Yu Wang, Bing Xie, Rui Tang, Hong-Yi Li, Kun Wen

"During present converter vanadium extraction process, phosphorus could not be removed from hot metal due to absence of CaO in slag though it is an efficient way for vanadium extraction. In order to improve the phosphorus remove and produce CaO-containing vanadium slag, which could be directly used in subsequent roasting process, during the converter vanadium extraction process, lime dissolution in FeOx-Si02-V203-Ti02 slag was investigated by using a rotating cylinder technique and the slag-lime interface was characterized by SEM/EDS. Results showed that changes in the slag chemistry and phase compositions during the lime dissolution process were similar to that in CaO-Si02-FeOx based slag during the BOF process. The V and Ti in the slag were expected to diffuse into the lattice of2CaO·Si02 solid solution, which formed a rather thinner layer in thickness at the slag-lime interface than that in BOF process, leading to improvement of lime dissolution in the slag.IntroductionVanadium is important material that widely applied in industries. The traditional technique to extract vanadium was to leach vanadium after sodium salt roasting. However, the sodium salt roasting process has several problems including lower yielding rate[!] and environmental pollution[2]. Therefore, the more environment-friendly technique of calcium roasting[3-4] was proposed. In order to increase roasting efficiency of vanadium slag, it is essential to study the dissolution/reaction mechanism between lime and vanadium slag. Many investigations about the dissolution reaction of lime in molten slag have been carried out from the standpoints of rapid slagging to De-Pin steelmaking process[5-6]. However, their studies were focused on BOF slag and the reaction mechanism between solid lime and slag containing vanadium has not been reported yet. In present work, the dissolution process was studied with rotating cylinder technique and the reaction interfaces were observed and analyzed by SEM/EDS to elucidate the dissolution mechanism of lime in vanadium slag. This work was supported by National Natural Science Foundation of China No. 51090382."

Jan 1, 2013

By Hong Yong Sohn

On the occasion of this symposium in my name, I reflect upon the contributions of my academic mentors and early associates who helped shape my professional career. I was fortunate to have these people around me during my graduate work and at the start of my professional career. In forming my view of the technical field and career, they represented academia, research institutions, industry, and different parts of the world.

Jan 1, 2006

By F. J. Tavera

The colloid flotation of lead carbonate precipitates in aqueous media is studied at a pH of 7. The flotation system consisted of five spargered flotation cells in a serial array. The flotation system was operated under controlled conditions of superficial air velocity, superficial liquid velocity, frother concentration, and collector concentration. The measured variables were gas hold-up, bubble size, superficial bubble surface flux, and lead recovery (reported to the concentrate). The experimental data show that it is possible to separate as much as 97% (w/w) lead from the aqueous media when the superficial gas velocity is 1 cm/s and the superficial liquid velocity is 0.19 cm/s.

Jan 1, 2006

By Adelana Adetunji

Ilmenite ore samples obtained from Dankoli in Zamfara, North Western Nigeria has been characterized using Energy Dispersive X-ray fluorescence (EDXRF) technique, X-ray diffraction (XRD) technique and the Neutron Activation Analysis (NAA) technique. The major constituents in the ore were quantitatively found to be TiO2 and Fe2O3 in concentrations of about 60wt% and 31wt% respectively. These occur in the forms of magnesian ilmenite (Fe, Mg)(Ti, Fe)O3, pure ilmenite (FeTiO3), and barium copper yttrium oxide (Ba2Cu3YO6.56) minerals. Other constituents/impurities in minor or trace quantities include MnO, Ta2O5, Nb2O5, Wo, SnO2, Hf, Zn, V, Zr, Co, Pb, Br, Al, Rb, Y, Th and U.

Jan 1, 2006

By M. Olper, M. Maccagni, C. J. N. Buisman, C. E. Schultz

The key point of the CX-EWS process is the conversion of lead compounds, contained in the active mass of spent batteries, into lead sulphide. The obtained lead sulphide is leached with ferric fluoborate electrolyte to dissolve lead and oxidize the sulphur from sulphide to the elemental form. The lead-rich solution is fed into a diaphragm electrolytic cell depositing lead and regenerating ferric fluoborate. The introduction of sulphate reducing bacteria technology in the sulphidization step of the battery paste improves dramatically the economics of the CXEWS process, reducing the costs of chemicals, avoiding gypsum disposal and minimising the unit operations of the process. This paper describes in detail this technology change with reference to the economics of the process.

Jan 1, 2000

By J. Miernik, D. Krupka, B. Ochab

The electrolytic zinc plant, with a capacity 75,000 tonnes per year, is part of Zaklady Gorniczo-Hutnicze BOLESLAW. It is the biggest zinc producer in Poland. The electrolytic zinc plant started up in 1955 with a capacity 15,000 tonnes per year, and multiplied its production by 5 till nowadays. At the beginning, the plant processed only calcine from zinc oxides (60% Zn, 3-4% Pb, 0,03 % Cd) which were produced from Waeltz fumes by calcination in a rotary kiln. Participation of calcine from zinc sulfide concentrates in the feed grew during the BOLESLAW plant expansion. Currently, only roasted sulphide concentrates, calcine from fluid-bed roasters, is processed. This paper presents a general description of the ZGH BOLESLAW plant and discusses the processes of roasting, leaching, purification and electrolysis. Also shown are the chemical analyses of the various process materials.

Jan 1, 2000

By D. A. R. Kay

Phase stability diagrams are used to predict the abilities of lanthanum and cerium oxides to desulfurize coal gasification products in the temperature range 800-1000 C. Results of desulfurization studies in laboratory fixed bed reactors illustrate the effects of i) sorbent preparation, ii) input gas quality and iii) temperature, on the desulfurization reaction. 2CeO(2-x)(s) + H2S(g) + (1-2x)H2 = Ce2O2S(s) + 2(1x)H2O(g) The results of desulfurization/oxidation regeneration cycles are also reported.

Jan 1, 1989

By Huang Rui

The coal asphalt is combusted at different temperature in a heating cabinet with the temperature limit by 1200°C. By comparing the mass of the remainder of each experiment, the completely combusting temperature of asphalt smoke can be determined. Based on the experimental process of asphalt smoke, a discrete mathematical model of the asphalt smoke combustion is set by theoretic analysis. Through computer programming, the dynamic combustion process of asphalt smoke is calculated to simulate the experimental model. The result of experiment shows that coal asphalt can mostly react upon 500°C and the mass of remainder is 49.41% to initial mass of sample in the condition. The computing result shows that the temperature and the concentration of asphalt smoke influence its burning temperature approximating linearity. The consumed quantity of fuel to ignite the asphalt smoke needs be considered with the two factors.

Jan 1, 2006

By Sunil Jayasekera

This paper describes the results of a study carried out to examine the feasibility of electrolytic recovery of silver from cyanide leach liquor generated from a Western Australian silver mine tailings using a novel high mass transfer electrowinning cell. The proposed circuit involves heap leaching and electrowinning in a closed loop. The filter-press-like closed electrode arrangement of the cell allowed much improved mass transfer of metal ions to the cathode surface, making direct electrowinning of metals from dilute solutions feasible. The tests were conducted both in the laboratory and at large scale using a prototype with ~1.0 m2 cathode area. The results showed that the recovery of silver from as low as 250 mg L-1tenor was feasible. The silver deposit produced with the prototype cell was non-adherent and powdery and could be readily removed from the closed cell. A system was developed so that silver powder was discharged continuously during the run.

Jan 1, 2003